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Tytuł pozycji:

An immunohistochemical assessment of cathepsin D in gastric carcinoma: its impact on clinical prognosis.

Tytuł:
An immunohistochemical assessment of cathepsin D in gastric carcinoma: its impact on clinical prognosis.
Autorzy:
Allgayer H; Department of Surgery, Klinikum Grosshadern, Ludwig Maximilians University of Munich, Germany.
Babic R
Grützner KU
Beyer BC
Tarabichi A
Wilhelm Schildberg F
Heiss MM
Źródło:
Cancer [Cancer] 1997 Jul 15; Vol. 80 (2), pp. 179-87.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: <2005- >: Hoboken, NJ : Wiley
Original Publication: New York [etc.] Published for the American Cancer Society by J. Wiley [etc.]
MeSH Terms:
Cathepsin D/*metabolism
Stomach Neoplasms/*metabolism
Stomach Neoplasms/*mortality
Adult ; Aged ; Aged, 80 and over ; Biomarkers ; Female ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Multivariate Analysis ; Plasminogen Activators/metabolism ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Risk Factors ; Serine Proteinase Inhibitors/metabolism ; Stomach Neoplasms/pathology ; Survival Analysis ; Urokinase-Type Plasminogen Activator/metabolism
Substance Nomenclature:
0 (Biomarkers)
0 (Serine Proteinase Inhibitors)
EC 3.4.21.- (Plasminogen Activators)
EC 3.4.21.73 (Urokinase-Type Plasminogen Activator)
EC 3.4.23.5 (Cathepsin D)
Entry Date(s):
Date Created: 19970715 Date Completed: 19970722 Latest Revision: 20220321
Update Code:
20240104
DOI:
10.1002/(sici)1097-0142(19970715)80:2<179::aid-cncr2>3.0.co;2-p
PMID:
9217027
Czasopismo naukowe
Background: In the context of tumor-associated proteolysis, the prognostic value of cathepsin D in breast carcinoma has been studied but its role is controversial in relation to gastrointestinal carcinoma. The aim of the current study was to determine whether cathepsin D is a prognostic parameter for gastric carcinoma, and also to consider interaction with the urokinase-plasminogen activator (uPA) system as an established risk factor for tumor-associated proteolysis.
Methods: In a consecutive prospective series of 203 gastric carcinoma patients, expression of cathepsin D in tumor cells was semiquantitatively analyzed with immunohistochemistry (scored 0-3). Median follow-up time was 31 months (range, 9-56 months). Kaplan-Meier (log rank) and multivariate Cox analyses were used to analyze survival.
Results: Kaplan-Meier analysis (log rank statistics) revealed significant association of increasing cathepsin D detection with poorer disease free survival (P = 0.0042) and poorer overall survival (P = 0.0018) of curatively resected patients. Overall survival of all patients was not significantly correlated. Multivariate analysis of established risk factors for gastric carcinoma, including the uPA system, identified cathepsin D as a new and independent prognostic parameter for disease free survival (P = 0.020; relative risk, 2.98; 95% confidence interval, 1.28-6.91). Plasminogen activator inhibitor type-1 as a representative of the uPA system was confirmed as a strong independent factor for disease free and overall survival. Chi-square analysis showed significant correlation of higher cathepsin D levels with Laurén's diffuse-type carcinomas and strong evidence of uPA receptor in tumor cells. However, a subgroup analysis performed according to Laurén's classification revealed a univariate prognostic impact of cathepsin D on both diffuse and intestinal types without independent value. For patients with high levels of uPA receptor (scores of 2 and 3, n = 132), a highly significant association of increasing evidence of cathepsin D with disease free survival (P < 0.0001) and overall survival (P < 0.0001) was observed for curatively resected patients. Significant association with survival was also observed for all patients (P = 0.0407).
Conclusions: Cathepsin D is a new functional prognostic parameter for gastric carcinoma patients with independent value for disease free survival. Moreover, this study indicates that consideration of more than one tumor-associated protease could lead to a more individualized estimation of risk for carcinoma patients.

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